Journal article
The synthesis of a cubane-substituted dipeptide
QI Churches, RJ Mulder, JM White, J Tsanaktsidis, PJ Duggan
Australian Journal of Chemistry | CSIRO PUBLISHING | Published : 2012
DOI: 10.1071/CH12179
Abstract
Amino acids and peptides bearing cyclic hydrocarbon side-chains are of interest in the development of a wide range of bioactive molecules. The preparation of an amino acid and a dipeptide derivative bearing an unfunctionalised cubane substituent is described. Attempts to prepare a cubylalanine derivative via the corresponding dehydroalanine were unsuccessful due to the high sensitivity of this vinyl cubane compound. Conversely, the addition of cubyllithium to a (RS)-glyoxylate sulfinimine led to an effective synthesis of a cubylglycine derivative and a cubane-substituted dipeptide in diastereomerically pure form. © CSIRO 2012.
Grants
Funding Acknowledgements
This work was funded by CSIRO's Preventative Health Flagship. Mike Falkiner and Chris Hallam, CSIRO Materials Science and Engineering, are thanked for providing dimethyl 1,4-cubanedicarboxylate.